HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925374Generated: October 28, 2026
5-Amino-2-naphthol → HCID 67520710, compound
https://huagongshe.com/reaction/1925374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Amino-2-naphthol | HCID 6865 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Iodo-1H-pyrazolo[3,4-b]pyridine | HCID 57642801 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67520710 | HCID 67520710 | — |
Reaction Steps
5-Aminonaphthalen-2-ol (356 mg, 2.24 mmol) was dissolved in DMF (2.5 mL) then cooled to 0° C. Sodium hydride (94 mg) was added slowly and the stirring was continued for 15 min at 0° C. 4-Iodo-1H-pyrazolo[3,4-b]pyridine (274 mg, 1.12 mmol) was then added slowly and the reaction was heated at 100° C. for 16 h, followed by 4.5 h at 120° C. The mixture was partitioned between water and EtOAc then washed with water, 1N aqueous NaOH, and brine. The organic layer was dried over sodium sulfate and concentrated in vacuo to give 6-(1H-pyrazolo[3,4-b]pyridin-4-yloxy)naphthalen-1-amine as a brown solid MS (ESI, pos. ion) m/z: 277.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178557B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-de8766272b96457f979e86217b40a156 |
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| Source note | uspto-grants-2012_05 |
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